Effects of Walking Apnea At Low Lung Volume on Hypoalgesia
1 other identifier
interventional
60
1 country
1
Brief Summary
The aim of this randomized controlled study is to explore the hypoalgesic response of a 6 minutes of intermittent walking apneas training session at low lung volume in healthy subjects; also, as secondary objectives, to analyze the cardiovascular and respiratory response produced during the intervention.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable pain
Started Nov 2024
Shorter than P25 for not_applicable pain
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
October 9, 2024
CompletedFirst Posted
Study publicly available on registry
October 15, 2024
CompletedStudy Start
First participant enrolled
November 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2025
CompletedOctober 15, 2024
October 1, 2024
6 months
October 9, 2024
October 9, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
Pain pressure threshold (PPT) on thumb, anterior tibial and spinous process of C7
PPT is tested on the dorsal base of the distal phalanx of the thumb on the dominant side and on the muscle belly of the tibialis anterior on the dominant side. The region to be pressed is marked with a pen. The patient is instructed to report with the first appearance of the sensation of "discomfort". An ascending ramp of 0.5 kg/cm/s is applied, at the rhythm of a metronome. The measurement is started on the thumb, and alternated with tibia and C7 until 3 measurements of each region are obtained, enough time to give 30 seconds of rest between measurements in the same region. This protocol has demonstrated high inter-observer reliability measuring healthy subjects (ICC = 0.91).
before and after intervention (up 30 minutes)
Secondary Outcomes (7)
Perceived Stress Scale (PSS)
before intervention (up 5 minutes)
Pittsburg Sleep Quality Index (PSQI)
before intervention (up 5 minutes)
Global Physical Activity Questionnaire (GPAQ)
before intervention (up 5 minutes)
Oxygen saturation
during intervention (up 6 minutes)
Blood pressure
before and after intervention (up 10 minutes)
- +2 more secondary outcomes
Study Arms (2)
Walking apnea at Low Lung Volume
EXPERIMENTALParticipants walk at 6 km/h (10% slope) on treadmill for 6 minutes performing series of intermitent apneas
Walking normal breathing
ACTIVE COMPARATORParticipants walk with normal breathing at 6 km/h (10% slope) on treadmill for 6 minutes.
Interventions
Walking apnea at low Lung Volume Participants walk at 6 km/h (10% slope) on treadmill for 6 minutes. Participants in the experimental group will perform intermittent apneas at high lung volume with a density of 5 seconds, followed by a normal breath of 5 seconds until completing the 6 minutes)
Participants walk at 6 km/h (10% slope) on treadmill for 6 minutes. Participants in the control group will remain breathing normally for these 6 minutes.
Eligibility Criteria
You may qualify if:
- Asymptomatic subjects aged between 18 and 64 years.
You may not qualify if:
- Cardiovascular, respiratory, metabolic, neurological or osteomuscular signs or pathologies.
- History of epilepsy.
- Pregnant
- Pharmacological treatment.
- Participants who present any type of pain on the day of the measurements or who have frequently suffered pain during the previous 4 weeks.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
CSEU LaSalle
Madrid, Spain
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Profesor / Investigador
Study Record Dates
First Submitted
October 9, 2024
First Posted
October 15, 2024
Study Start
November 1, 2024
Primary Completion
May 1, 2025
Study Completion
May 1, 2025
Last Updated
October 15, 2024
Record last verified: 2024-10
Data Sharing
- IPD Sharing
- Will not share